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Haloalkanes and Haloarenes

JEE Main 2026 (Online) 28th January Evening ShiftMCQEasy📈 Topic in 11% papers+4−1
Ques. 1JEE Main 2026, 28 January (Evening Shift)

Identify the correct statements : The presence of -NO2 group in benzene ring Choose the correct answer from the options given below :

  1. A and D Only
  2. B and D Only
  3. C and A Only
  4. B and C Only

Answer

(4) B and C Only

Solution

-NO2 is strongly electron-withdrawing (−I and −R effects).

It decreases the electron density of the ring (especially at o- and p-positions), so the ring is deactivated towards electrophilic substitution B true, A false.

In nucleophilic substitution, an o-/p-NO2 group stabilises the negatively charged intermediate (carbanion) by resonance, so the ring is activated towards nucleophilic substitution (as per NCERT, o/p-nitrochlorobenzenes react easily with OH-) C true, D false.

B and C only

Answer: (4)

Keep practising — Haloalkanes and Haloarenes

Ques. 2JEE Main 2026, 24 January (Morning Shift)

Given below are two statements : In the light of the above statements, choose the correct answer from the options given below

  1. Statement I is false but Statement II is true
  2. Statement I is true but Statement II is false
  3. Both Statement I and Statement II are true
  4. Both Statement I and Statement II are false
Ques. 3JEE Main 2026, 24 January (Morning Shift)

Match the List-I with List-II Choose the correct answer from the options given below :

  1. A-III, B-IV, C-I, D-II
  2. A-IV, B-I, C-III, D-II
  3. A-III, B-IV, C-II, D-I
  4. A-I, B-II, C-IV, D-III
Ques. 4JEE Main 2026, 22 January (Morning Shift)

As compared with chlorocyclohexane, which of the following statements correctly apply to chlorobenzene? Choose the correct answer from the options given below :

  1. B, C and E Only
  2. A, C and E Only
  3. B, C and D Only
  4. A, D and E Only
Ques. 5JEE Main 2026, 22 January (Morning Shift)

The correct order of the rate of reaction of the following reactants with nucleophile by SN1 mechanism is : (Given : Structures I and II are rigid) [figure]

  1. I < II < III < IV
  2. II < I < III < IV
  3. III < I < II < IV
  4. IV < III < II < I
Ques. 6JEE Main 2026, 22 January (Morning Shift)

The correct order of reactivity of CH3Br in methanol with the following nucleophiles is F-, I-, C2H5O- and C6H5O-

  1. I- > C2H5O- > C6H5O- > F-
  2. I- > F- > C6H5O- > C2H5O-
  3. I- > C6H5O- > F- > C2H5O-
  4. I- > C2H5O- > F- > C6H5O-
Ques. 7JEE Main 2026, 21 January (Evening Shift)

The correct order of the rate of the reaction for the following reaction with respect to nucleophiles is : CH3Br + Nu- CH3Nu + Br-

  1. ClO4- > CH3COO- > OH- > PhO-
  2. OH- > PhO- > CH3COO- > ClO4-
  3. CH3COO- > PhO- > OH- > ClO4-
  4. PhO- > OH- > CH3COO- > ClO4-
Ques. 8JEE Main 2026, 21 January (Evening Shift)

The correct order of reactivity of the following benzyl halides towards reaction with KCN is : [figure]

  1. a > b > c > d
  2. b > a > d > c
  3. b > a > c > d
  4. a > b > d > c
Ques. 9JEE Main 2025, 7 April (Morning Shift)

The reactions which cannot be applied to prepare an alkene by elimination, are Choose the correct answer from the options given below:

  1. B & E Only
  2. B, C & D Only
  3. A, C & D Only
  4. B & D Only
Ques. 10JEE Main 2025, 7 April (Evening Shift)

Match List - I with List - II. Choose the correct answer from the options given below :

  1. A-II, B-III, C-I, D-IV
  2. A-III, B-IV, C-II, D-I
  3. A-IV, B-III, C-I, D-II
  4. A-IV, B-III, C-II, D-I
Ques. 11JEE Main 2025, 4 April (Evening Shift)

Given below are two statements : In the light of the above statements, choose the most appropriate answer from the options given below :

  1. Both Statement I and Statement II are incorrect
  2. Both Statement I and Statement II are correct
  3. Statement I is incorrect but Statement II is correct
  4. Statement I is correct but Statement II is incorrect

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